Canonical Allele Identifier: CA1548139585
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882403G= , CM000667.2:g.56882403G= GRCh38
NC_000005.9:g.56178230G= , CM000667.1:g.56178230G= GRCh37
NC_000005.8:g.56213987G= NCBI36
NG_031884.1:g.72331G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3203G= MANE Select ENSP00000382423.3:p.Gly1068=
ENST00000399503.3:c.3203G= ENSP00000382423.3:p.Gly1068=
NM_005921.1:c.3203G= NP_005912.1:p.Gly1068=
XM_005248519.3:c.2825G= XP_005248576.2:p.Gly942=
XM_011543406.1:c.2948G= XP_011541708.1:p.Gly983=
XM_011543407.1:c.2924G= XP_011541709.1:p.Gly975=
XM_011543408.1:c.3203G= XP_011541710.1:p.Gly1068=
XM_017009484.1:c.2792G= XP_016864973.1:p.Gly931=
XM_017009485.1:c.2714G= XP_016864974.1:p.Gly905=
XR_001742068.2:n.3234G=
NM_005921.2:c.3203G= MANE Select NP_005912.1:p.Gly1068=